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Master Production Record Requirements - Webinar By GlobalCompliancePanel

20 December 2011, Wilmington, United States


Introduction
This webinar will address the 21CFR and Eudralex Volume 4 requirements and interpretation, as well as FDA Guidance regarding the creation, review and approval, and control of Master Production Records.
Venue
Online Training

Online Training, 1000 N West Street, DE, Suite 1200, Wilmington, 19801, United States

Organised by
Global compliance panel
Contact information
Mr webinars web
online training webinar, 1000 N West Street, Suite 1200, Wilmington, 19801, United States of America
8004479407
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